Canonical Allele Identifier: CA510290455

Gene: GSS

Linked Data

• MyVariant Identifiers: chr20:g.33519826G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34932023G>C , CM000682.2:g.34932023G>C	GRCh38
NC_000020.10:g.33519826G>C , CM000682.1:g.33519826G>C	GRCh37
NC_000020.9:g.32983487G>C	NCBI36
NG_008848.1:g.28776C>G
NG_008848.2:g.29005C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642498.1:c.945C>G	ENSP00000493631.1:p.Gly315=
ENST00000642538.1:c.*289C>G	ENSP00000493927.1:n.*289C>G
ENST00000643188.1:c.945C>G	ENSP00000493903.1:p.Gly315=
ENST00000643443.1:c.*652C>G	ENSP00000495572.1:n.*652C>G
ENST00000643502.1:c.602C>G
ENST00000643908.1:n.1163C>G
ENST00000644538.1:n.1222C>G
ENST00000644793.1:c.945C>G	ENSP00000495750.1:p.Gly315=
ENST00000645328.1:c.323C>G
ENST00000645408.1:c.478C>G
ENST00000645723.1:n.2184C>G
ENST00000646405.1:c.*363C>G	ENSP00000493744.1:n.*363C>G
ENST00000646497.1:n.890C>G
ENST00000646512.1:n.1091C>G
ENST00000646735.1:c.612C>G	ENSP00000493763.1:p.Gly204=
ENST00000651619.1:c.945C>G MANE Select	ENSP00000498303.1:p.Gly315=
ENST00000216951.6:c.945C>G	ENSP00000216951.2:p.Gly315=
ENST00000451957.2:c.612C>G	ENSP00000407517.2:p.Gly204=
NM_000178.2:c.945C>G	NP_000169.1:p.Gly315=
XM_005260406.3:c.945C>G	XP_005260463.1:p.Gly315=
XM_011528796.1:c.945C>G	XP_011527098.1:p.Gly315=
NM_000178.4:c.945C>G MANE Select	NP_000169.1:p.Gly315=
NM_001322494.1:c.945C>G	NP_001309423.1:p.Gly315=
NM_001322495.1:c.945C>G	NP_001309424.1:p.Gly315=